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African Journal of Biotechnology Vol. 9(46), pp. 7948-7954, 15 November, 2010 Available online at http://www.academicjournals.

org/AJB ISSN 16845315 2010 Academic Journals

Full Length Research Paper

Evaluation of antioxidant potential of medicinal plants from Malaysian Rubiaceae (subfamily Rubioideae)
Ahmad R.1*, Mahbob E. N. M.1, Noor Z. M.1, Ismail N. H.1, Lajis, N. H.2 and Shaari K.2
1

Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia. 2 Institute of Bioscience, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Accepted 27 September, 2010

This paper evaluates the antioxidant potential of 22 species of medicinal plants from Malaysian Rubiaceae. The ferric thiocyanate (FTC), thiobarbituric acid (TBA), total phenolic content (TPC) and the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assays were employed. The tested extracts showed strong antioxidant potential when compared to butylated hydroxytoluene (BHT), quercetin and vitamin E with percent inhibition of 91 - 99% in the FTC, and 77 - 97% in the TBA assays. The TPC of extracts found varied from 8.55 to 120.63 mgGAE/gPE. Psychotria griffithii and Hydnophytum formicarum showed total phenolic content of more than 100 mgGAE/gPE and strong DPPH radical-scavenging activity with IC50 values of 14.0 and 22.4 g/ml, respectively. The standard vitamin C and BHT showed IC50 values of 12.8, and 5.6 g/ml, respectively. A good correlation was observed between total phenolic content and radical-scavenging activities. The medicinal plants in this study tested are expected to be good sources of natural antioxidants. Key words: Antioxidant, Rubiaceae, ferric thiocyanate (FTC), thiobarbituric acid (TBA), 1,1-diphenyl-2picrylhydrazyl (DPPH), total phenolic content (TPC). INTRODUCTION With 10700 species distributed in 637 genera, the Rubiaceae represents one of the largest plant family which mainly consists of tropical woody plants. They also grow as trees, shrubs or less often as perennial to annual herbs, as in Rubieae (subfamily Rubioideae) which are found in temperate regions. The most recent and complete classification based on molecular, morphological and chemical evidence has subdivided this family into four subfamilies, including Cinchonoideae, Ixoroideae, Antirheoideae and Rubioideae (Mongrand et al., 2004). Most of the species in this family have been used widely by various indigenous people and particularly, by traditional practitioners as remedies. Among the common ones are species from the genera Hedyotis, Ophiorrhiza and Psychotria. In Malaysia, reports on Rubiaceous plants include phytochemical and pharmacological studies on Mitragyna, Uncaria and our own work on Morinda and Hedyotis species (Ahmad et al., 2005; Houghton et al., 1991; Ismail et al., 1997; Kam et al., 1992; Takayama et al., 2001). Some Hedyotis species are used as ingredients in Chinese herbal medicines for the treatment of cancer, and the medicine namely peh-hue-juwa-chicao contains Hedyotis diffusa as one of the active components (Ahmad et al., 2005). Another species, Hedyotis hedyotideae, is also a medicinal herb used in the treatment of colds, stomatitis and various inflammations. Pharmacological studies of ethanolic extracts of this plant revealed that it possesses an anti-ulcer effect. A full review on the phytochemical studies and pharmacological activities of plants in genus Hedyotis (formerly known as Oldenlandia) has been recently documented (Lajis and Ahmad, 2006). Numerous phytochemical and pharmacological studies

*Corresponding author. E-mail: rohayaahmad@ salam.uitm.edu.my. Tel: +603-55444565. Fax:+60355444562. Abbreviations: FTC, Ferric thiocyanate; TBA, thiobarbituric acid; DPPH, 1,1-diphenyl-2-picrylhydrazyl; TPC, total phenolic content; OD, optical density; AOA, antioxidant activity; BHT, butylated hydroxytoluene; PTDC, pyrrolidinedithiocarbamate; TNF, tumor necrosis factor- .

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carried out on herbaceous plants have resulted in the development of natural antioxidants (Balunas and Kinghorn, 2005). According to Shahidi (1997), antioxidants are known to act at different levels in the oxidative sequence in the body. They may act by decreasing oxygen concentration, intercepting singlet oxygen, preventing first-chain initiation by scavenging initial radicals such hydroxyl radicals, binding metal ion catalysts, decomposing primary products to non-radical compounds, and chain-reaction breaking to prevent continued hydrogen abstraction from substrates. Various methods have been used to evaluate and compare the antioxidant activity in an attempt to provide a meaningful interpretation relating to health. In this study, we evaluate the antioxidant activity of plants via their inhibition of lipid peroxidation in a biochemical system and investigate the radical-scavenging activities (via the DPPH method) as a further method of evaluating antioxidant activity. Phenolic phytochemicals are secondary metabolites of plant origin which constitute one of the most abundant groups of natural metabolites and are synthesized by plants in order to protect themselves from biological and environmental stresses. Recent studies have shown that phenolic compounds possess high antioxidant activity and certain therapeutic properties, including anti-diabetic and anti-hypertension activity (Apostolidis et al., 2007). Thus, the determination of total phenolic content may be used as an indirect evaluation of the antioxidant potential of the extracts. In the first phase of our study, we reported the antioxidant and other biological activities of seven Hedyotis species and other Rubiaceous plants (Ahmad et al., 2005; Saha et al., 2004). However, towards a chemotaxonomic study of the antioxidant potential of Rubiaceae family, screening of more plants is necessary. Thus, the second phase of our study is the antioxidant screening of 22 species of Malaysian Rubiaceae with a focus on the subfamily Rubioideae. The 22 species from 10 genera and their local name in parenthesis include Argostemma sp., Argostemma yappii, Chasalia minor, Chasalia pubescens, Hedyotis corymbosa, Hedyotis philippinensis (lidah jin), Hedyotis havilandi, Hydnophytum formicarum (kelapa berok/naga stong), Lasianthus cyanocarpus, Lasianthus maingayi (telinga rusa), Lasianthus pilosus, Ophiorrhiza major (sebueh bukit), Ophiorrhiza discolor, Psychotria griffithii (bunga mempitit), Psychotria lasiocaphala, Psychotria ophirensis, Rennellia elliptica, Spermacoce exilis, Spermacoce latifolia, Urophyllum ferrugineum, Urophyllum glabrum and Urophyllum griffithianum.
MATERIALS AND METHODS Plant material Plant samples were collected from various parts of Peninsular Malaysia. Voucher specimens were deposited at the herbarium of

the Laboratory of Natural Product, Institute of Bioscience, Universiti Putra Malaysia, Serdang, Selangor, Malaysia. Sample preparation and extraction Leaves, stems or whole samples were cut into small pieces, airdried in the shade and ground into fine powder before being extracted with methanol. Extracts were evaporated to dryness under reduced pressure before being subjected to the antioxidant assays. Antioxidant activity Antioxidant activities were evaluated by the inhibition of lipid peroxidation in the ferric thiocyanate (FTC) and thiobarbituric acid (TBA) assays. FTC and TBA assays were carried out as described previously (Ahmad et al., 2005). Total phenolic content (TPC) of extract was estimated by the Folin-Ciocalteu assay (Kumaran and Karunakaran, 2007), while the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay is as described in Saha et al. (2004) with slight modification. The strength of radical scavenging property was evaluated via the reduction in the optical density (OD) of DPPH at 517 nm. As cited by Abas et al. (2006), extract with an IC50 value of less than 30 g/ml, between 30 - 100 g/ml and more than 100 g/ml is considered to possess strong, moderate, and weak free radicalscavenging activity, respectively.

RESULTS AND DISCUSSION In the search of new therapeutic agents from natural sources, especially from medicinal plants, various direct and indirect approaches have been applied to determine their antioxidant activity (AOA). In this study, the antioxidant potential of methanolic extracts of Malaysian Rubiaceae, particularly the subfamily Rubioideae, was evaluated using the complementary FTC and TBA assays. These methods are based on the effect of extracts on the inhibition of lipid peroxidation in a biochemical system. Since antioxidant activity is often correlated to the total phenolic contents (Jayaprakasha et al., 2008; Kaur et al., 2008), the Folin-Ciocalteu assay was used to obtain an estimation of the total phenolic content. To further evaluate the antioxidant potential, we also employed the DPPH method. The DPPH assay measures the ability of antioxidants to scavenge free radicals which is not directly associated with the real oxidative degradation or effects of transient metals (Roginsky and Lissi, 2005). In the FTC assay, all tested extracts (Figure 1) showed lower absorbance values when compared to the control with high AOA and percent inhibition of 91.7 - 98.5% (Table 1) which is comparable to those of butylated hydroxytoluene (BHT), vitamin E and quercetin. The absorbance values for H. formicarum and P. griffithii is further shown as an inset in Figure 1 along with the absorbance values for BHT, vitamin E and quercetin. In the TBA assay, a similar trend was observed with all tested extracts exhibiting low absorbance values correlating to a percent inhibition of 77.3 - 97.3%. The

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Figure 1. Antioxidant activity of crude methanolic extracts of 22 Rubiaceous species as measured by the FTC method.

standards, BHT, vitamin E and quercetin showed a slightly lower inhibition of 93.5, 85.6 and 91.4%, respectively, when compared to the values in the FTC. Almost all samples and standards in TBA showed slightly lower percent inhibitions than those obtained in FTC. The difference could indicate that the amount of peroxide in the initial stages of lipid peroxidation (as measured by

FTC) is relatively higher than the amount of secondary products in the later stages (as measured by TBA). The comparison of the AOA observed for the plant samples and the three standards between the two methods is shown in Table 1. In the Folin-Ciocalteu assay, the content of total phenolics in Rubiaceous plant extracts determined using

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Table 1. A comparison between antioxidant activity (AOA) of crude methanolic extracts of 22 Rubiaceous species by FTC and TBA methods.

Sample* Argostemma sp. Argostemma yappii Chasalia minor Chasalia pubescens Hedyotis havilandi Hedyotis philippinensis (leaves) Hedyotis philippinensis (stems) Hydnophytum formicarum Lasianthus cyanocarpus Lasianthus maingayi Lasianthus pilosus Ophiorrhiza discolor Ophiorrhiza major Psychotria griffithii Psychotria lasiocaphala Psychotria ophirensis Rennellia elliptica Spermacoce exilis Spermacoce latifolia Urophyllum ferrugineum Urophyllum glabrum Urophyllum griffithianum BHT Quercetin Vitamin E
*Final concentration of 0.02% (w/v).

Absorbance on final day FTC 0.1757 0.0792 0.0815 0.0313 0.0647 0.0865 0.0430 0.0321 0.7950 0.0835 0.0672 0.0971 0.0470 0.0389 0.0647 0.0501 0.0456 0.0378 0.0759 0.0576 0.0423 0.0550 0.0397 0.1302 0.2213

AOA (% inhibition) FTC 91.7 96.3 96.2 98.5 96.9 95.9 97.9 98.5 96.3 96.1 96.8 95.4 97.8 98.2 96.9 97.6 97.8 98.2 96.4 97.3 98.0 97.4 98.1 93.9 89.6

Absorbance on final day TBA 0.5713 0.2121 0.1217 0.1629 0.1265 0.1391 0.2877 0.2084 0.3228 0.2145 0.2934 0.3828 0.1220 0.1630 0.1879 0.3243 0.0828 0.1164 0.5935 0.1784 0.1195 0.0714 0.1702 0.2245 0.2462

AOA (% inhibition) TBA 78.1 91.9 95.3 93.8 95.2 94.7 88.9 92.0 87.7 91.8 88.3 85.4 95.3 93.8 92.8 87.6 96.8 95.5 77.3 93.2 95.1 97.3 93.5 91.4 85.6

the linear regression equation varied from 8.55 to 120.63 mgGAE/gPE. The results (Table 2) revealed that H. formicarum possessed the highest amount of total phenolics with 120.63 3.09 mgGAE/gPE followed by P. griffithii with 102.46 0.96 mgGAE/gPE, respectively. The lowest phenolic content was found in L. pilosus with 8.55 2.50 mgGAE/gPE. Based on the FTC and TBA assays, high percentage of inhibition observed towards lipid oxidation indicated strong antioxidant potential and may be correlated to the total phenolics in the plant extracts which may be in the form of flavonoids, simple phenolics, terpenes or tannins. While the FTC and TBA assays are non-specific, the DPPH radical-scavenging are mechanism-based. In the DPPH method, the antioxidant potential of the plant extracts was assessed on the basis of their scavenging activity of the stable DPPH free radical. Among the samples tested (Table 2), the extracts of P. griffithii and H. formicarum were found to be strong free radical scavengers with IC50 values of 14.0 and 22.4 g/ml, respectively in comparison with vitamin C (5.6 g/ml) and BHT (12.8 g/ml). As shown in Table 2, the activity found

correlates well with the results of the TPC assay in which both extracts were found to contain high amounts of total phenolics which has been correlated with the number of hydrogen donating groups in the phenolic compounds (Kaur et al., 2008). However, moderate activity was found for U. griffithianum and weak activities were found for P. ophirensis, H. philippinensis (leaves and stems) and R. elliptica with IC50 values of 43 - 227 g/ml. The high AOA of the extracts could justify well their use as traditional remedies. Generally, all of the tested plants have been used by the Malays as well as Chinese community for medicinal purposes, either internally or externally. Some are used as poultice to treat snakebites, broken bones, bruises, rheumatism, lumbago, ague and skin disorders such as eczema. Internally, a decoction of some plants is given for constipation, indigestion, heartburn, gastric verigo, dysentery, gonorrhoea and also as a tonic (Burkill, 1966) and taken after childbirth. The role of flavonoids as antioxidants has been wellestablished and there have been numerous reports on structure-activity relationships in the last decade (Abas et al., 2006; Rastija and Medic-Saric, 2008). Among the

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Table 2. DPPH free radical-scavenging activity vs. total phenolic contents of 22 Rubiaceous species (in the order of increasing radical scavenging activity).

Sample Lasianthus cyanocarpus Lasianthus pilosus Hedyotis corymbosa Argostemma yappii Ophiorrhiza discolor Hedyotis havilandi Chassalia pubescens Psychotria lasiocaphala Lasianthus maingayi Spermacoce latifolia Urophyllum glabrum Argostemma cf. viscidum Ophiorrhiza major Chassalia minor Spermacoce exilis Urophyllum ferrugineum Rennellia elliptica Hedyotis philippinensis (stems) Psychotria ophirensis Hedyotis philippinensis (leaves) Urophyllum griffithianum Hydnophytum formicarum Psychotria griffithii BHT Vitamin C Quercetin

IC50 value ( g/ml (DPPH) Na Na Na Na Na Na Na Na Na Na Na Na Na Na Na Na 227.244.31 130.784.35 116.222.89 114.190.34 43.242.60 22.401.73 13.993.25 12.812.31 5.590.64 Nd

Radical-scavenging property (DPPH) weak weak weak weak moderate strong strong strong strong strong

Total phenolics (mgGAE/gPE) (Folin Ciocalteu) 8.61 1.02 8.55 2.50 10.98 0.16 11.39 0.93 13.11 0.17 12.26 1.18 12.54 0.92 13.90 2.36 14.03 2.77 17.00 0.35 15.60 2.44 18.54 0.66 20.41 0.23 15.77 4.98 27.57 1.71 27.59 2.49 19.48 0.93 9.76 0.81 21.76 0.45 9.27 0.02 25.23 1.85 120.63 3.09 102.46 0.96 -

The data represent the meansstandard deviation (SD) of triplicates of three independent experiments. Significance analysis was performed by ANOVA (P < 0.05). Na, Not active; Nd, not detectable in experimental concentration range (250 - 3.90 g/ml); strong radicalscavenging activity, IC50 < 30 g/ml; moderate radical-scavenging activity, 30 g/ml IC50 100 g/ml; weak radical-scavenging activity, a IC50 > 100 g/ml (Abas et al., 2006); data presented are means of two replicates from two independent experiments.

extracts tested, flavonoids have only been reported in the genus Hedyotis and H. formicarum, while none has been documented for the other genera (Lajis and Ahmad, 2006; Prachayasittikul et al., 2008). However, since other natural products such as iridoid glycosides and indole alkaloids are also abundant in this subfamily, it is yet to be ascertained whether the antioxidant potential reported can be attributed to the flavonoids alone, or to any of the other natural products, or to a synergistic effect of the compounds present. Iridoid glycosides have long been known to be of chemotaxonomic significance in the subfamily Rubioideae (Inouye et al., 1988; Lopes et al., 2004). These iridoids have shown various activities such as antitumoral, hemodynamic, chloretic and hepatoprotective. Loganin, for example, isolated from Palicourea rigida from the tribe Psychotrieae exhibited high efficacy as an anti-inflammatory agent. In other studies, preliminary evaluation in treating rheumatoid arthritis showed that the iridoids

asperuloside and deacetyl asperulosidic acid from Lasianthus acuminatissimus exhibited an inhibitory effect on the release of tumor necrosis factor- (TNF-) from cultured mouse peritoneal macrophages with IC50 values of 0.52 and 1 g/ml, respectively (Recio et al., 1993). Indole alkaloids represent another class of compounds found in abundance in this family. In A. yappii, an indole alkaloid (+)-isochimonanthine has been isolated from the leaves of the plant (Hibino and Choshi, 2002). Similarly, in Psychotria and Ophiorrhiza species, the isolation of indole alkaloids such as psychollatine from Psychotria umbellata and ophiorrhizine from O. major has been reported (Arbain et al., 1992; Fragoso et al., 2008). Although the antioxidant activity of indole alkaloids isolated from these genera are not known, Saha et al. (2004) have reported the cytotoxic effects of Psychotria rostrata against RAW 264.7 macrophage cells at a concentration of 250 g/ml. In a separate study, schischkiniin, an indole alkaloid isolated from the seeds

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of Centaurea schischkinii (Asteraceae) has shown significant antioxidant activity against the DPPH free radical with an IC50 value of 3.8 g/ml (Shoeb et al., 2005). The bioactive indole alkaloid camptothecin (found in Ophiorrhiza pumila) has been reported to act as stimuli in inducing the metal chelator pyrrolidinedithiocarbamate (PTDC) to protect UV-irradiated human leukemia cell line (HL-60 cells) from apoptosis. In this respect, camptothecin may be regarded as an antioxidant since apoptosis has been associated with oxidative stress and antioxidant pathways have been suggested to play a central role in the protection against it (Verhaegen et al., 1995). The compound has also been found to show inhibitory activity against tumor cells by blocking the eukaryotic topoisomerase as well as against HIV-1 (Kitajima et al., 2003). To the best of our knowledge, no phytochemical study has been done on 17 out of 22 species tested. Phytochemical studies have only been reported for A. yappii, H. formicarum, H. corymbosa, O. discolor and O. major. Phytochemical study of H. formicarum (which has been found to be active in the four assays) has yielded bioactive flavonoid and phenolic compounds: isoliquiritigenin, butin, butein, stigmasterol and protocatechualdehyde. It is conceivable that the potent antioxidative and radical-scavenging activities of H. formicarum may result from these constituents and could explain its reported effect on cancer cells (Itharat and Ooraiku, 2007; Prachayasittikul et al., 2008). Although no phytochemical study has been reported for P. griffithii, based on previous chemotaxonomic studies, it is expected that flavonoids, iridoids and indole alkaloids are present. For R. elliptica, P. ophirensis and H. philippinensis (leaves and stems), the weak activities found should not be a deterrent in investigating the plant in consideration of the kinetics of DPPH reaction (Bondet et al., 1997). This study, therefore, warrants phytochemical investigations on the six plants in order to investigate the bioactive constituents responsible for its antioxidant activity. In conclusion, based on the inhibition of lipid peroxidation via the FTC and TBA assays, the methanolic extracts of all plant species tested were found to possess strong antioxidant potential. Taking into account the results of all four assays including the TPC and the DPPH assays, six plants namely, H. formicarum, P. griffithii, U. griffithianum, P. ophirensis, H. philippinensis (leaves and stems) and R. elliptica are expected to be good sources of natural antioxidants. Fractionation of extracts based on polarity and subsequent screening of the fractions would be the next logical step. Since most plants tested are used to treat rheumatism and antiinflammatory-related diseases, screening of extracts for anti-inflammatory properties such as inhibitory effect on the release of TNF- or inhibition of nitric oxide production will be a part of our future studies. The findings will hopefully help to explain the mechanism of antioxidant action and lead to the characterisation of new and interesting antioxidant principle which could combat oxi-

dative stress leading to diseases like diabetes, hypertension, inflammation and cancer. It is anticipated that a correlation between the antioxidant activities of plants in the Rubiaceae family (particularly the subfamily Rubioideae) and its active principles could be established. ACKNOWLEDGEMENTS The authors would like to thank the Ministry of Higher Education (MOHE) of Malaysia and Research Management Institute (RMI) of Universiti Teknologi MARA (UiTM) for research grants no. 600-IRDC/ST/ FRGS 5/3/1247 and 600-RMI/ST/FRGS 5/3/FST (35/2009). Appreciation also goes to Dr Shamsul Khamis of Institute of Bioscience, Universiti Putra Malaysia (UPM) for collection and identification of plants.
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